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相关概念视频

The Replisome03:01

The Replisome

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DNA replication is carried out by a large complex of proteins that act in a coordinated matter to achieve high-fidelity DNA replication. Together this complex is known as the DNA replication machinery or the replisome.
The synthesis of the leading and lagging strands is a highly coordinated process. To explain this, the “Trombone model” was proposed by Bruce Alberts in 1980. The DNA loop formation starts when a primer is synthesized on the parent lagging strand. The loop grows with...
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Restarting Stalled Replication Forks02:37

Restarting Stalled Replication Forks

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DNA replication is initiated at sites containing predefined DNA sequences known as origins of replication. DNA is unwound at these sites by the minichromosome maintenance (MCM) helicase and other factors such as Cdc45 and the associated GINS complex.The unwound single strands are protected by replication protein A (RPA) until DNA polymerase starts synthesizing DNA at the 5’ end of the strand in the same direction as the replication fork. To prevent the replication fork from falling apart,...
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Molecular Chaperones and Protein Folding03:00

Molecular Chaperones and Protein Folding

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The native conformation of a protein is formed by interactions between the side chains of its constituent amino acids. When the amino acids cannot form these interactions, the protein cannot fold by itself and needs chaperones. Notably, chaperones do not relay any additional information required for the folding of polypeptides; the native conformation of a protein is determined solely by its amino acid sequence. Chaperones catalyze protein folding without being a part of the folded protein.
The...
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Translesion DNA Polymerases02:10

Translesion DNA Polymerases

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Translesion (TLS) polymerases rescue stalled DNA polymerases at sites of damaged bases by replacing the replicative polymerase and installing a nucleotide across the damaged site. Doing so, TLS allows additional time for the cell to repair the damage before resuming regular DNA replication.
TLS polymerases are found in all three domains of life - archaea, bacteria, and eukaryotes. Of the different classes of TLS polymerases, members of the Y family are fitted with specialized structures that...
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DNA Helicases00:55

DNA Helicases

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DNA unwinding helicase enzymes are a type of motor protein. Motor proteins can translocate along filaments or polymers using energy generated from ATP hydrolysis. Helicases are involved in all the important cellular processes where DNA unwinding is required, such as DNA replication, repair, recombination, and transcription. They are present in all living organisms, but vary in their structure, function, and mechanism of action. For example, in prokaryotes, DnaB helicase binds and translocates...
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Homologous Recombination02:31

Homologous Recombination

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The basic reaction of homologous recombination (HR) involves two chromatids that contain DNA sequences sharing a significant stretch of identity. One of these sequences uses a strand from another as a template to synthesize DNA in an enzyme-catalyzed reaction. The final product is a novel amalgamation of the two substrates. To ensure an accurate recombination of sequences, HR is restricted to the S and G2 phases of the cell cycle. At these stages, the DNA has been replicated already and the...
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Updated: Jun 6, 2025

Chemical Triphosphorylation of Oligonucleotides
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折叠器和自我复制器之间的光介导互转换

Yulong Jin1,2, Pradeep K Mandal3, Juntian Wu4

  • 1Beijing National Laboratory for Molecular Sciences, CAS Key Laboratory of Analytical Chemistry for Living Biosystems, Institute of Chemistry, Chinese Academy of Sciences, 100190 Beijing, China.

Journal of the American Chemical Society
|November 26, 2024
PubMed
概括
此摘要是机器生成的。

这项研究表明,单个分子构建块如何在实验室环境中形成自复制纤维或折叠分子 (折叠分子). 外部刺激,如和pH值的变化, 控制了结构的形成, 提供了关于生命起源的见解.

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Internalization and Observation of Fluorescent Biomolecules in Living Microorganisms via Electroporation
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科学领域:

  • 生命研究的起源
  • 超分子化学
  • 系统化学

背景情况:

  • 自复制分子和折叠的宏分子对于生命的出现和进化至关重要.
  • 在非生物系统中这些结构之间的相互作用尚未得到充分理解.

研究的目的:

  • 展示一个单一的构建块可以形成自复制分子或折叠体的非生物系统.
  • 调查控制这些独特结构形成的刺激.

主要方法:

  • 使用基于二硫化物的动态组合库.
  • 应用机械激发和控制的pH条件.
  • 引入光酸以操纵光的pH值.

主要成果:

  • 在和中等pH下选择性形成的单一构造块自复制的六合体纤维.
  • 一种15个子单元的宏环折叠剂,在较低的pH值或没有动时形成并积累.
  • 通过外部刺激,包括光引起的pH变化,实现了折叠器和自我复制器之间的相互转换.

结论:

  • 从单个前体产生自我复制或折叠体的可控非生物系统.
  • 展示了包括光在内的外部刺激在这些状态之间的转变的潜力.
  • 为了解生命早期复杂性和消散性结构的出现提供了一个模型系统.